"MLYCD" Related Products

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Recombinant Human MLYCD cell lysate

Cat.No.: MLYCD-1119HCL
Description: The product of this gene catalyzes the breakdown of malonyl-CoA to acetyl-CoA and carbon dioxide. Malonyl-CoA is an intermediate in fatty acid biosynthesis, and also inhibits the transport of fatty acyl CoAs into mitochondria. Consequently, the encoded protein acts to increase the rate of fatty acid oxidation. It is found in mitochondria, peroxisomes, and the cytoplasm. Mutations in this gene result in malonyl-CoA decarboyxlase deficiency.
Species: Human
Size: 100 ul
Storage Buffer: 1X Sample Buffer (50 mM Tris-HCl, 2% SDS, 10% glycerol, 300 mM 2-mercaptoethanol, 0.01% Bromophenol blue)
Applications: Western Blot;
Gene Name: MLYCD malonyl-CoA decarboxylase [ Homo sapiens ]
Official Symbol: MLYCD
Synonyms: MLYCD; malonyl-CoA decarboxylase; malonyl-CoA decarboxylase, mitochondrial; hMCD; MCD; malonyl coenzyme A decarboxylase; MGC59795;
Gene ID: 23417
mRNA Refseq: NM_012213
Protein Refseq: NP_036345
MIM: 606761
UniProt ID: O95822
Chromosome Location: 16q24
Pathway: Malonate semialdehyde pathway, propanoyl-CoA =>Acetyl-CoA, organism-specific biosystem; Malonate semialdehyde pathway, propanoyl-CoA => Acetyl-CoA, conserved biosystem; Metabolic pathways, organism-specific biosystem; Peroxisome, organism-specific biosystem; Peroxisome, conserved biosystem;
Function: lyase activity; malonyl-CoA decarboxylase activity;

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